Showing entry for Cataract, total congenital with posterior sutural opacities in Heterozygotes

General Disease Information
BXGD Id	BXGD021911
Disease Name	Cataract, total congenital with posterior sutural opacities in Heterozygotes
Disease CUI Id	C4049005
MeSH Codes	C16   C11
Disease Class Name	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases
Semantic Type	Congenital Abnormality
Human Phenotype Ontology Id
Human Phenotype Ontology Term
Disease Ontology Id	DOID:630   DOID:7
Disease Ontology Class Name	genetic disease; disease of anatomical entity
Disorder Network	disorder-protein-compound-food associations